子类
医学
免疫学
抗体
免疫系统
人类白细胞抗原
表位
自身免疫性疾病
疾病
多发性硬化
补体系统
结缔组织
抗原
病理
作者
Maartje G. Huijbers,Luís Querol,Erik H. Niks,Jaap J. Plomp,Silvère M. van der Maarel,Francesc Graus,Josep Dalmau,Isabel Illa,Jan J.G.M. Verschuuren
摘要
At least 13 different disease entities affecting the central nervous system, peripheral nervous system and connective tissue of the skin or kidneys are associated with immunoglobulin G4 (IgG4) immune reactivity. IgG4 has always been considered a benign, non-inflammatory subclass of IgG, in contrast to the well-known complement-activating pro-inflammatory IgG1 subclass. A comprehensive review of these IgG4 autoimmune disorders reveals striking similarities in epitope binding and human leukocyte antigen (HLA) associations. Mechanical interference of extracellular ligand-receptor interactions by the associated IgG4 antibodies seems to be the common/converging disease mechanism in these disorders.
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